EP2956574B1 - Agencement d'anode à diffusion de gaz hydrogène pour la production d'hcl - Google Patents

Agencement d'anode à diffusion de gaz hydrogène pour la production d'hcl Download PDF

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EP2956574B1
EP2956574B1 EP14751509.2A EP14751509A EP2956574B1 EP 2956574 B1 EP2956574 B1 EP 2956574B1 EP 14751509 A EP14751509 A EP 14751509A EP 2956574 B1 EP2956574 B1 EP 2956574B1
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Prior art keywords
anode
gas
hcl
arrangement
electrolysis
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German (de)
English (en)
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EP2956574A1 (fr
EP2956574A4 (fr
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Joël FOURNIER
Lionel ROUÈ
Sébastien HELLE
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Alliance Magnesium
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Alliance Magnesium
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    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
    • C25C7/02—Electrodes; Connections thereof
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/01—Products
    • C25B1/24—Halogens or compounds thereof
    • C25B1/26—Chlorine; Compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
    • C25C1/02—Electrolytic production, recovery or refining of metals by electrolysis of solutions of light metals
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/04—Electrolytic production, recovery or refining of metals by electrolysis of melts of magnesium
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/06—Electrolytic production, recovery or refining of metals by electrolysis of melts of aluminium
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
    • C25C7/02—Electrodes; Connections thereof
    • C25C7/025—Electrodes; Connections thereof used in cells for the electrolysis of melts
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
    • C25C7/06—Operating or servicing

Definitions

  • the present description relates to an hydrogen gas diffusion anode arrangement for use in electrolytic production of metals such as magnesium and aluminum producing hydrogen chloride (HCl) as a by-product.
  • metals such as magnesium and aluminum producing hydrogen chloride (HCl) as a by-product.
  • Aluminum and magnesium are common structural metal with high commercial interest.
  • Al Pure aluminum
  • Al is a silver-white, malleable, ductile metal with one-third the density of steel. It is the most abundant metal in the earth's crust. Aluminum is an excellent conductor of electricity and has twice the electrical conductance of copper. It is also an efficient conductor of heat and a good reflector of light and radiant heat.
  • aluminum does not occur in its native state, but occurs ubiquitously in the environment as silicates, oxides and hydroxides, in combination with other elements such as sodium and fluoride, and as complexes with organic matter. When combined with water and other trace elements, it produces the main ore of aluminum known as bauxite.
  • Magnesium compounds primarily magnesium oxide (MgO), are used as a refractory material in furnace linings for producing iron, steel, nonferrous metals, glass and cement. Magnesium oxide and other magnesium compounds are also used in the agricultural, chemical, automobile, aerospace and construction industries.
  • aluminum is produced by separating pure alumina from bauxite in a refinery, then treating the alumina by electrolysis using the Hall-Heroult and Bayer processes.
  • the Bayer process and the Hall-Heroult process together have been the standard commercial method of the production of aluminum metal. These processes require large amounts of electricity and generate undesired by products, such as fluorides in the case of the Hall-Heroult process and red mud in the case of the Bayer process.
  • an anode arrangement for use in an electrolysis production of metals comprising an anode having a hollow body comprising a cavity extending longitudinally from a first end portion to a second end portion of the anode, said body having at least one gas outlet connected in fluid flow communication with the cavity; a gas inlet connected in fluid flow communication with the cavity of said anode, said gas inlet being connectable to a source of hydrogen gas for feeding hydrogen gas into the cavity of said anode; an electrical connector for generating a current at the anode during electrolysis; and a hydrogen chloride (HCI) recuperator surrounding at least a portion of the anode for recovering HCI gas released through the at least one gas outlet at an outer surface of the anode during electrolysis, the HCI recuperator having an outlet connectable to a HCI redistributor.
  • HCI hydrogen chloride
  • the first end portion is a top portion of the anode and the second end portion is a bottom portion of the anode, the gas inlet connected to the top portion or bottom portion of the anode.
  • the electrical connector extends into the cavity of the anode.
  • the electrical connector extends into the gas inlet into the cavity of the anode.
  • the metals are magnesium or aluminum.
  • the anode is a cylindrical anode.
  • the anode comprises a plurality of gas outlets symmetrically spaced on the body of the anode.
  • the size of the gas outlets increases from the top portion of the anode to the bottom portion of the anode.
  • the gas outlets are spaced in rows and columns on the body of the anode.
  • each gas outlets within each row are of the same size.
  • the gas outlets are cylindrical bores.
  • the gas outlets are elongated taper channels from the bottom portion to the top portion of the anode.
  • the anode is a metal diffuser.
  • the anode is made of sintered metal powders.
  • the anode is made of graphite or Hastalloy X.
  • the gas inlet is the HCl recuperator, extending partially and surrounding at least a portion of the anode recovering HCl gas released through the gas outlet at the outer surface of the anode during electrolysis.
  • the HCl recuperator is a sintered alumina tube.
  • the at least one gas outlet as an opening of at least 5 ⁇ m.
  • the anode described herein further comprises an electrocatalyst.
  • an electrolytic cell for electrolyzing metals chloride comprising, the anode arrangement as described herein; a cathode being separated from the anode, the HCl gas released through the gas outlet at the outer surface of the anode is separated from the metals produced at the cathode; and an electrolytic chamber containing an electrolyte, said cathode and said anode arrangement.
  • anode arrangement for use in an electrolysis production of aluminum comprising an anode having a hollow body comprising a cavity extending longitudinally from a first end portion to a second end portion of the anode, said body having at least one gas outlet connected in fluid flow communication with the cavity; a gas inlet connected in fluid flow communication with the cavity of said anode, said gas inlet being connectable to a source of hydrogen gas for feeding hydrogen gas into the cavity of said anode; an electrical connector for generating a current at the anode during electrolysis; and a hydrogen chloride (HCl) recuperator surrounding at least a portion of the anode for recovering HCl gas released through the at least one gas outlet at an outer surface of the anode during electrolysis, the HCl recuperator having an outlet connectable to a HCl redistributor.
  • HCl hydrogen chloride
  • an anode arrangement for use in an electrolysis production of magnesium comprising an anode having a hollow body comprising a cavity extending longitudinally from a first end portion to a second end portion of the anode, said body having at least one gas outlet connected in fluid flow communication with the cavity; a gas inlet connected in fluid flow communication with the cavity of said anode, said gas inlet being connectable to a source of hydrogen gas for feeding hydrogen gas into the cavity of said anode; an electrical connector for generating a current at the anode during electrolysis; and a hydrogen chloride (HCl) recuperator surrounding at least a portion of the anode for recovering HCl gas released through the at least one gas outlet at an outer surface of the anode during electrolysis, the HCl recuperator having an outlet connectable to a HCl redistributor.
  • HCl hydrogen chloride
  • the anode described herein can be used in extraction processes of magnesium and aluminum using hydrochloric acid which is recycled during the processes as described in International Application No. PCT/CA2013/050659 and in U.S. Patent Application No. 61/827709, filed May 27, 2013 .
  • the anode is immersed into molten salt electrolyte and the HCl gas generated at the surface goes on the top of the cell.
  • the cell is generally fed with an inert gas in order to prevent oxygen contact with the molten metal.
  • the HCl is therein mixed with this inert gas. This very dry mixture is leaving the cell at 700°C and could be used as a drying agent for the conversion for example of MgCl 2 -hydrate brine into MgCl 2 prill.
  • the gas is then pass throw a water scrubber (HCl redistributor) device where the HCl gas is convert to HCl liquid and the inert gas is return to the electrolytic cell after a drying step.
  • the HCl liquid concentration is adjusted by the number of pass of the liquid in contact with the HCl charged mixing gas. When the concentration reach 32%wt, the HCl liquid solution is flush to be return to the tank and fresh water is introduce into the scrubber.
  • Magnesium and aluminum are presently isolated using electrolytic processes.
  • the electrolytic reduction of molten magnesium chloride (MgCl 2 ) is a commonly used process for the production of magnesium.
  • MgCl 2 molten magnesium chloride
  • Two major problems are related to this process.
  • the production of magnesium requires a huge quantity of energy. Based on the free Gibbs energy of formation, a minimum power of 5.5 kWh is required for the production of 1 kg of Mg.
  • the different resistance components electrolyte, bubbles, and electrodes
  • U.S. Patent Pub. No. 2002/0014416 describes the use of a high surface area anode, the anode being porous and to which hydrogen gas is fed, to produce magnesium metal by electrolysis of magnesium chloride.
  • the design of the anode in the 2002/0014416 publication does not take into account the variance in the hydrostatic pressure exerted by the molten magnesium chloride in the electrolytic cell (prior to electrolysis). Because the anode is a vertical cell, the hydrostatic pressure exerted by the molten magnesium chloride is greater at the bottom of the anode than at the top of the anode. The hydrostatic pressure thus starts at a particular value near the top of the anode and increases towards the bottom of the anode where it is greatest.
  • an anode such as that of the 2002/0014416 publication (wherein the channels or pores- as the case may- are similar and equally spaced around and up-and-down across the anode) yields a structure where more hydrogen gas will exit the anode at the top (where the hydrostatic pressure is less) than will exit at the bottom (where the hydrostatic pressure is greater). This results (depending on the pressure and volume of the hydrogen gas in the cavity of the anode) either in an insufficient amount of hydrogen gas exiting the anode near the bottom or an excess amount of hydrogen gas exiting near the top. Neither situation is ideal.
  • the anode described herein is part of an assembly that allows recuperation of HCl produced. Further, the anode described herein contains channel/pore volume which are varied to compensate for the variance in the hydrostatic pressure presented by molten magnesium for example.
  • the anode disclosed herein nearer to the top of the anode (where the hydrostatic pressure is less) the anode comprises a smaller channel/pore volume. Nearer to the bottom of the anode (where the hydrostatic pressure is greater) the anode comprises a greater channel/pore volume.
  • the channel/pore volume will progressively increase as one progresses down the length of the anode from top to bottom.
  • the channel/pore volume can be calculated and will increase proportionally with the increase in hydrostatic pressure - thus attempting to ensure that substantially the same amount of hydrogen gas exits the anode across its external surface area whatever the distance be from the top/bottom of the anode. This results in a sufficient amount of hydrogen gas exiting the anode, reducing or eliminating the attack by chlorine gas on the carbon in the anode, reducing or eliminating the production of chlorinated carbon compounds, reducing or eliminating the production of chlorine gas and substituting therefor the production of hydrogen chloride gas, and reducing the voltage required with respect to the electrolysis of the magnesium chloride or aluminum chloride without requiring an excess of hydrogen gas.
  • the reversible decomposition voltage works out to be about 1.8 volts.
  • MgCl 2 decomposes into liquid magnesium at the cathode and gaseous chlorine at the anode according to the Eq. 1.
  • the theoretical voltage of the reaction is 2.50 V.
  • the decomposition voltage decreases to 1.46 V, allowing a theoretical voltage reduction of about 1V, the overall cell voltage could reach a reduction of 0.86 V. This represents a reduction of 25% in energy consumption.
  • HCl as by-product of the process. Since the purification process of MgCl 2 and AlCl 3 ores consumes gaseous HCl for the dehydration step, this is of great interest to produce on-site the HCl required for this process. This lead to economic benefits and a simplification of the process because the amount of HCI produced by electrolysis should be sufficient to feed the chemical reactor for the dehydration process. The theoretical amount of HCl which can be produced during magnesium electrolysis can be estimated from Eq.
  • FIG. 1 it is shown in an embodiment an anode 10 as encompassed herein.
  • Anodes for the electrolysis could be made, as encompassed herein, of a self-sustaining matrix of sintered powders of at least one oxy-compound such a soxides, multipleoxides, mixed oxides, oxyhalides and oxycarbides, of at least one metal selected from the group consisting of lanthanum, terbium, erbium, ytterbium, thorium, titanium, zirconium, hafnium, niobium, chromium and tantalum and at least one electroconductive agent, the anode being provided over at least a portion of its surface with at least one electrocatalyst for the electrolysis reaction and bipolar electrodes for the cells which electrodes are resistant to corrosion in molten salt electrolysis and have a good electroconductive and good electrocatalytic activity.
  • the anode 10 has an elongated body 12.
  • the body 12 can be made of graphite for example, preferably porous graphite.
  • the body can be of any shape, such has being cylindrical.
  • the shape of the anode ideally needs to be easy to machine, present a homogenous gas distribution at its surface and fit easily with electrochemical cell components.
  • the anode body can be a metal diffuser, fabricated from sintered metal powders, leading to interconnected porosity through which the gas is able to diffuse.
  • the bubbles generated at the surface are homogeneously distributed and their size can be easily varied with the pore diameter.
  • Sintered metal diffusers are available in a large choice of materials and in different ranges of porosity, such as for example Hastalloy X. Pore size of as low as 5 ⁇ m can be used in such metal diffuser.
  • the anode 10 is inserted in a tube 22 consisting of a HCI recuperator closed at one extremity by a cap 26.
  • the HCl recuperator 22 is for example a sintered alumina tube of 1 inch.
  • the cap 26 can be a T-shape Swagelok fitting as depicted in Fig. 1 .
  • the gas bubble 20 produced at the surface of the anode 10 stay constrain inside the alumina tube and have no other choice than going up inside the HCl recuperator 22.
  • the anodic gases 20 are separated from the magnesium or aluminum produced at the cathode preventing any back reaction. Gases 20 formed at the anode are then transferred into a HCl redistributor through the gas outlet 27.
  • a bubbler is used to recuperate the HCl gas through the gas outlet 27 in order to measure the level of HCl produced.
  • the bubbler can be filled with a NaOH solution.
  • An acid-base titration of the NaOH solution after electrolysis is performed for the quantification of the produced HCl.
  • the anode 10 Within the body 12 of the anode 10, there is a longitudinal cavity 14 (as seen in Fig. 2 ) to which is connected a gas inlet connector 18 for feeding hydrogen gas.
  • the gas inlet 18 can be connected for example on top of the anode 10 or at the bottom of the anode 10. When connected at the bottom of the anode 10, the hydrogen gas can be bubbled in the anode 10 from the gas inlet 18.
  • the gas inlet 18 can be protected by the HCI recuperator 22.
  • the gas inlet connector 18 can be made of stainless still and can also act as a HCl recuperator. Accordingly, the HCl recuperator 22 and the gas inlet connector 18 can be the same tube.
  • the anode 10 further comprises an electrical connector 16 passing through the gas inlet through the longitudinal cavity of the anode 10 ( Fig. 2 ).
  • the anode 110 connected to a gas inlet 118 comprise, along the body 112, are a series of channels 120.
  • the channels 120 extend from the exterior surface of the body 112 to the longitudinal cavity 114 ( Fig. 3B ).
  • the channels 120 thus form a series of gas outlets.
  • the channels are arranged generally symmetrically around the body 112 in a series of row 124 and columns 126.
  • the channels 120 are formed as right circular cylindrical bores in the body 112.
  • each row 124 e.g. within row 124a
  • each of the channels 120 has generally the same volume (e.g. the diameter of each channel 120 is basically the same).
  • an anode 210 connected to a gas inlet 218 having an elongated right circular cylindrical body 212 made of graphite.
  • the body 212 comprises a series of channels 220.
  • the channels 220 thus form a series of gas outlets.
  • the channels 220 are arranged generally symmetrically around the body 212, extending from the exterior surface of the body 212 to the longitudinal cavity 214.
  • the channels 220 are elongate and taper from the bottom 230 to the top 228 of the body 212.
  • Each channel 220 (labels as 226a, 226b, 226c, etc.) is generally of the same size and shape.
  • the hydrogen anode can be further modified by maximizing the gas diffusion through the graphitic anode.
  • the incorporation of an electrocatalyst in the anode to decrease the overpotential for H 2 oxidation and thus the cell voltage is also encompassed.
  • the second type of hydrogen gas diffusion anode evaluated was a metal diffuser.
  • This anode was fabricated from sintered metal powders, made of Hastalloy X, leading to interconnected porosity through which the gas is able to diffuse.
  • Such an anode is very attractive because the bubbles generated at the surface are homogeneously distributed and their size can be easily varied with the pore diameter.
  • the finest available pore size of about 5 ⁇ m were chosen.
  • the pore distribution size could be adapted along the surface to take into account the hydrostatic pressure variation from top to bottom of the electrolytic cell.
  • porous graphite anodes were evaluated. This kind of electrode consist of a graphite rod drilled along its axis in order to give wall thickness of about 1/8". To prevent any H 2 leaks at the gas inlet connector tube/graphite interface, the upper part of the graphite electrode was machined to give exactly the same diameter than the inside diameter of the gas inlet connector tube. Then, the lowermost part of the gas inlet connector tube was heated leading to its thermal expansion, allowing the graphite electrode to be inserted. During cooling, the gas inlet connector tube contracted around the graphite electrode leading to a strong and leak-free connection between the two parts. To protect the stainless tube against corrosion appearing close to the gas inlet connector tube/graphite interface, this area was protected by a sintered alumina tube while the upper part was protected by alumina cement.
  • the graphitisation level for synthetic grahite determine the level of orientation of graphite plan among the cross section of the anode. This graphitization level is the result of parameter such as temperature, pressure and reaction time while anode manufacturing. This property could be use to control the chaneling-porosity along the anode for hydrostatic pressure control.
  • Electrochemical measurements were conducted at 700°C with the apparatus for the gas capture as described previously. Electrolysis test conducted at 0.5 A.cm -2 for one hour with an Ar-5%H 2 flow rate of 845 cm 3 .min -1 demonstrated a stable behavior as shown in Fig. 5 .
  • the cell voltage is around 4.0 V. The short time variation of the voltage with a maximum amplitude 0.1V can be attributed to the high gas flow rate. These perturbations were not observed with a lower flow rate (e.g., 376 cm 3 min -1 ).
  • the lower cell voltage observed in this case, compared to an electrolysis without hydrogen is due to a lower current density and most of all, by the fact that alumina tube surrounding the anode causes a lower resistance than the separation wall.
  • Electrochemical measurements were realized with an anode made of Hastalloy X generally employed to resist to high temperature corrosive environments. Compared to the previous type of electrode, sintered metal diffusers have the advantage of diffusing gas very homogeneously. Thus, hydrogen bubbles generated at the anode surface are very small and well distributed. Chronopotentiometric measurements were carried out with different flow rates of Ar-5%H 2 and at various current densities. The evolution of the cell voltage with the gas flow rate for different current densities is plotted in Fig. 7 . For all current densities, a slight decrease of the cell voltage reduction is observed at a low gas flow rate (65-145 cm 3 min -1 ).
  • Porous graphite represents the most promising type of hydrogen anodes for magnesium electrolysis tested. No noticeable trace of corrosion were found on the carbon anodes. Thus, it appears that carbon represents an ideal choice of anode material for magnesium electrolysis because of its excellent corrosion resistance at high temperature in MgCl 2 based molten salt. In addition, it was observed that hydrogen was capable of diffusing through the electrode wall providing a good distribution of small bubbles at the surface of the electrode. However, the first tests were conducted with a carbon rod in which the hydrogen seems to diffuse preferentially along the axis of the rod leading to a higher concentration of bubbles at the bottom part of the electrode.
  • the anodic oxidation of H 2 must be favored for instance by increase the effective surface area of the anode (resulting in a decrease of the current density) or/and by adding an electrocatalyst for H 2 oxidation (resulting in a decrease of the anodic overpotential).
  • the conversion efficiency was calculated by comparing the amount of HCI produced during electrolysis with the amount of HCl theoretically produced.
  • the amount of hydrogen gas injected through the anode is controlled by a flow meter.
  • the flow rate can be easily corrected by using a conversion table.
  • the accuracy of a ball flow meter is limited to ⁇ 1-2 cm 3 min -1 which therefore has a slight influence on the calculation of the theoretical produced HCl. Assuming that the amount of HCl which can be produced only depends on the H 2 flow rate, the theoretical molar flow rate of produced HCl follow a linear law as represented by the black solid line in Fig. 9 .
  • the theoretical production of Cl 2 can be calculated from the faraday law which depends on the anodic current. After calculation, it can be found that for a current density of 0.5 A cm -2 , the amount of produced Cl 2 is in excess for H 2 flow rates of 9 and 18 cm 3 min -1 and is equimolar for 30 cm 3 min -1 . At 0.5 A cm -2 and for all studied flow rates, the reaction is only limited by the H 2 flow rate.
  • Figs. 9A-B represent the experimental data of the produced HCl quantified by acid - base titration.
  • a current density of 0.5 A cm -2 ( Fig. 9A )
  • the quantity of produced HCl increases as the H 2 flow rate increases up to 18 cm 3 min -1 and furthermore is very close to the theoretical line, indicating a high efficiency of conversion.
  • the conversion efficiency was found to be comprised between 77 and 85%.
  • the HCl production does not increase and as a consequence, the efficiency of conversion drastically decreases to about 50-60 %.
  • the plateau observed after 18 cm 3 min -1 can be related to the faradic yield of the Mg electrolysis reaction.
  • the conversion efficiency of the process is very high, between 80 and almost 100%.
  • the relatively poor faradic yield of the Mg electrolysis observed during the tests should not be seen as an end since industrial electrolysis cells usually run with faradic yield by far higher thanks to their optimized design and operation conditions. In this way, if assumed that a faradic yield of 90% and a conversion efficiency of 90% can be obtained in an industrial cell, it can be estimated that about 365 kg h -1 of HCl could be produced by an electrochemical cell running at 300kA.
  • FIG. 10 shows the two electrodes under a gas flow rate of 30 cm 3 .min -1 during a bubbling test into water.
  • the electrode with preferential gas diffusion along the anode axis presents a large bubble on the bottom part of the rod with smaller bubbles dispersed around the cylinder.
  • the bubble dispersion is more homogeneous.
  • Such an electrode presents a superior number of smaller bubbles surrounding the overall surface. On the lowermost part, no large bubbles were observed but only small ones. Note that the bubble homogeneity could be further increased by using a carbon with smaller size of pores.

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Claims (15)

  1. Agencement d'anode pour une utilisation dans une production de métaux par électrolyse comprenant :
    une anode présentant un corps creux comprenant une cavité s'étendant longitudinalement à partir d'une première portion d'extrémité vers une seconde portion d'extrémité de l'anode, ledit corps présentant au moins une sortie de gaz connectée en communication fluidique avec la cavité ;
    une entrée de gaz connectée en communication fluidique avec la cavité de ladite anode, ladite entrée de gaz pouvant être connectée à une source de gaz hydrogène pour une alimentation de gaz hydrogène dans la cavité de ladite anode ;
    un connecteur électrique pour une génération d'un courant au niveau de l'anode pendant une électrolyse ; et
    un récupérateur de chlorure d'hydrogène (HCl) entourant au moins une portion de l'anode pour une récupération de gaz HCl libéré à travers l'au moins une sortie de gaz au niveau d'une surface externe de l'anode pendant une électrolyse, ledit récupérateur de HCl présentant une sortie pouvant être connectée à un redistributeur d'HCl.
  2. Agencement d'anode selon la revendication 1, dans lequel la première portion d'extrémité est une portion supérieure de l'anode et la seconde portion d'extrémité est une portion inférieure de l'anode, l'entrée de gaz connectée à ladite portion supérieure ou portion inférieure de l'anode.
  3. Agencement d'anode selon la revendication 1 ou 2, dans lequel le connecteur électrique s'étend dans la cavité de ladite anode.
  4. Agencement d'anode selon la revendication 3, dans lequel ledit connecteur électrique s'étendant dans l'entrée de gaz dans la cavité de ladite anode.
  5. Agencement d'anode selon l'une quelconque des revendications 1 à 4, dans lequel lesdits métaux sont du magnésium ou de l'aluminium.
  6. Agencement d'anode selon l'une quelconque des revendications 1 à 5, dans lequel ladite anode est une anode cylindrique.
  7. Agencement d'anode selon l'une quelconque des revendications 1 à 6, dans lequel ladite anode comprend une pluralité de sorties de gaz symétriquement espacées sur le corps de ladite anode.
  8. Agencement d'anode selon l'une quelconque des revendications 1 à 7, dans lequel ladite anode est un diffuseur de métal.
  9. Agencement d'anode selon l'une quelconque des revendications 1 à 8, dans lequel ladite anode est composée de poudres métalliques frittées.
  10. Agencement d'anode selon l'une quelconque des revendications 1 à 9, dans lequel ladite anode est composée de graphite ou d'Hastalloy X.
  11. Agencement d'anode selon l'une quelconque des revendications 1 à 10, dans lequel l'entrée de gaz est le récupérateur d'HCl, s'étendant partiellement et entourant au moins une portion de l'anode récupérant du gaz HCl libéré à travers la sortie de gaz au niveau de la surface externe de l'anode pendant une électrolyse.
  12. Agencement d'anode selon l'une quelconque des revendications 1 à 11, dans lequel le récupérateur d'HCl est un tube d'alumine fritté.
  13. Agencement d'anode selon l'une quelconque des revendications 1 à 12, dans lequel l'au moins une sortie de gaz a une ouverture d'au moins 5 µm.
  14. Agencement d'anode selon l'une quelconque des revendications 1 à 13, comprenant en outre un électrocatalyseur dans l'anode.
  15. Cellule électrolytique pour une électrolyse de chlorure de métaux comprenant,
    l'agencement d'anode selon l'une quelconque des revendications 1 à 14 ;
    une cathode étant séparée de l'anode, le gaz HCl libéré à travers la sortie de gaz au niveau de la surface externe de l'anode est séparé des métaux produits au niveau de la cathode ;
    et une chambre électrolytique contenant un électrolyte, ladite cathode et ledit agencement d'anode.
EP14751509.2A 2013-02-14 2014-02-14 Agencement d'anode à diffusion de gaz hydrogène pour la production d'hcl Active EP2956574B1 (fr)

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US201361764711P 2013-02-14 2013-02-14
PCT/CA2014/050102 WO2014124539A1 (fr) 2013-02-14 2014-02-14 Agencement d'anode à diffusion de gaz hydrogène pour la production d'hcl

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EP3141621A1 (fr) 2011-05-04 2017-03-15 Orbite Aluminae Inc. Procédés de récupération de terres rares dans divers minerais
CA2848751C (fr) 2011-09-16 2020-04-21 Orbite Aluminae Inc. Procedes de preparation d'alumine et de divers autres produits
BR112014016732A8 (pt) 2012-01-10 2017-07-04 Orbite Aluminae Inc processos para tratar lama vermelha
WO2013142957A1 (fr) 2012-03-29 2013-10-03 Orbite Aluminae Inc. Procédés de traitement de cendres volantes
MY175471A (en) 2012-07-12 2020-06-29 Orbite Tech Inc Processes for preparing titanium oxide and various other products
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EP2956574A1 (fr) 2015-12-23
EA201591416A1 (ru) 2015-12-30
CA2889797C (fr) 2016-04-12
EP2956574A4 (fr) 2016-11-02
AU2014218302A1 (en) 2015-09-03
US10151040B2 (en) 2018-12-11
CN105026620A (zh) 2015-11-04
EA029037B1 (ru) 2018-01-31
BR112015019408A2 (pt) 2017-07-18
UA117473C2 (uk) 2018-08-10
GEP20186858B (en) 2018-06-11
KR20150126607A (ko) 2015-11-12
WO2014124539A1 (fr) 2014-08-21
BR112015019408B1 (pt) 2021-09-21
AU2014218302B2 (en) 2018-07-19
CN105026620B (zh) 2018-04-24
EA201591416A8 (ru) 2017-10-31
JP6465816B2 (ja) 2019-02-06
CA2889797A1 (fr) 2014-08-21
US20150345038A1 (en) 2015-12-03
JP2016510362A (ja) 2016-04-07
KR102260211B1 (ko) 2021-06-02

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